Predict the number of signals expected (disregarding splitting) in the 'H NMR spectrum of the compound shown below. (HINT: the solvent is CDCI3 and the O- H resonance "disappears") CH3 HO CH3 А. З В. 4 С. 5 D. 6

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**Predict the Number of ¹H NMR Signals**

**Question:**  
Predict the number of signals expected (disregarding splitting) in the ¹H NMR spectrum of the compound shown below.  
**HINT:** The solvent is CDCl₃ and the O-H resonance "disappears."

![Structure of Compound](image_placeholder)  

- **Compound Structure:** The depicted compound is a molecule with an alcohol group (HO) attached to a carbon chain with two methyl groups (CH₃) and one ethyl group (CH₃CH₂).

**Options:**  
A. 3  
B. 4  
C. 5  
D. 6  
E. 7  

**Choices:**  

- ○ D
- ○ E
- ○ A
- ○ C
- ○ B

The goal is to identify the number of distinct proton environments, which correspond to the number of signals in the ¹H NMR spectrum, excluding the OH proton due to the solvent's effect.
Transcribed Image Text:**Predict the Number of ¹H NMR Signals** **Question:** Predict the number of signals expected (disregarding splitting) in the ¹H NMR spectrum of the compound shown below. **HINT:** The solvent is CDCl₃ and the O-H resonance "disappears." ![Structure of Compound](image_placeholder) - **Compound Structure:** The depicted compound is a molecule with an alcohol group (HO) attached to a carbon chain with two methyl groups (CH₃) and one ethyl group (CH₃CH₂). **Options:** A. 3 B. 4 C. 5 D. 6 E. 7 **Choices:** - ○ D - ○ E - ○ A - ○ C - ○ B The goal is to identify the number of distinct proton environments, which correspond to the number of signals in the ¹H NMR spectrum, excluding the OH proton due to the solvent's effect.
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